Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- befree-2016 importedOn "2016-02-19" NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_assertion wasGeneratedBy ECO_0000203 NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_assertion wasDerivedFrom befree-2016 NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_assertion SIO_000772 21881542 NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_assertion evidence source_evidence_literature NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.
- NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_assertion description "[In this study, we explored the contribution of two DCDC2 markers to dyslexia, related reading and memory phenotypes in nuclear families of Italian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920587.RABtQAvJUCljwHorqWvwGmXfktr_Cs7vvK4NYf5w3kPmE130_provenance.